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正增塑剂在橡胶胶料中起着重要作用。可用来改善未硫化胶料的加工性能、自粘性、分散和流动性能。增塑剂可降低硫化胶的模量或改善其低温性能,或使用便宜的油或填料填充聚合物来降低橡胶胶料的成本,主增塑剂可溶解橡胶,促进聚合物链的布朗运动,从而降低胶料的粘度。助增塑剂不能溶解弹性体,但它们可在聚合物链间起润滑剂的作用以改善流动性。选择增塑剂时,很重 相似文献
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研究新型环保橡胶助剂增塑剂D810、分散剂WBP-100、助交联剂Ricobond 1756和改性酚醛树脂对氢化丁腈橡胶(HNBR)性能的影响及其在HNBR汽车同步带胶料中的应用。结果表明:增塑剂D810可有效代替传统增塑剂TOTM和TP-95用于HNBR中;分散剂WBP-100可改善HNBR的拉伸性能,提高硫化效率,在一定程度上延长HNBR汽车同步带的使用寿命;助交联剂Ricobond1756用量为2.5份可改善HNBR胶料的拉伸性能,使HNBR汽车同步带动态疲劳寿命延长约13%;新型改性酚醛树脂可有效提高HNBR胶料与尼龙帆布和玻璃纤维线绳的粘合性能。 相似文献
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研究高芳烃含量的环烷基环保橡胶增塑剂HJA0810(以下简称增塑剂HJA0810)在工业橡胶板胶料中的应用,并与现用机油进行对比。结果表明:与添加机油的胶料相比,添加增塑剂HJA0810的胶料混炼工艺性能和硫化特性相当,硫化胶的物理性能和耐热老化性能提高;随着增塑剂HJA0810用量增大,硫化胶的物理性能和耐热老化性能提高,耐压缩疲劳性能先提高后降低;增塑剂HJA0810可等量或适当增量替代机油应用于工业橡胶板胶料中,改善工业橡胶板胶料的环保性能。 相似文献
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研究新型环保橡胶助剂增塑剂D810、分散剂WBP-100、助交联剂Ricobond 1756和改性酚醛树脂对氢化丁腈橡胶(HNBR)性能的影响及其在HNBR汽车同步带中的应用。结果表明:增塑剂D810可有效代替传统增塑剂TOTM和TP-95用于HNBR中;分散剂WBP-100可改善HNBR的拉伸性能和耐热老化性能,提高硫化效率,在一定程度上延长HNBR汽车同步带的使用寿命;助交联剂Ricobond1756用量为2.5份可改善HNBR胶料的拉伸性能,汽车同步带动态疲劳寿命延长约13%;新型改性酚醛树脂可有效提高HNBR胶料与尼龙帆布和玻璃纤维线绳的粘合性能。 相似文献
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研究了二烯类热塑性聚氨酯在橡胶胶料中的应用性能。Poly bd 2035 TPU树脂可用作中间粘合层来粘合聚氨酯和其他橡胶材料;也可作为添加剂加入到胶料中,能在提高粘合性能的同时,改善生胶的加工性能、提高生胶强度、降低滞后性能,以及改善耐疲劳龟裂性能。 相似文献
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Sara P. Fore H. P. Pastor J. P. Hughes W. G. Bickford 《Journal of the American Oil Chemists' Society》1960,37(8):387-390
Summary Ten maleinated jojoba oil derivatives were screened as plasticizers in a standard polyvinyl resin formulation and as softeners
for Buna-N rubber. Three of these, the methyl and butyl esters and hydrogenated methyl esters of maleinated jojoba acids,
were comparable to the reference standard, DOP, as primary plasticizers for the vinyl resin. Three others were satisfactory
only as secondary plasticizers. Six of the derivatives were comparable to the reference softener, dibutyl sebacate, as softeners
in a Buna-N formulation and yielded rubbers meeting the low temperature flexibility requirements (−40°C.) of the automotive
industry. Two of the six, those made with the butyl and hydrogenated butyl esters of maleinated jojoba acids, met the still
more stringent low-temperature requirements of the aircraft industry (−55°C.).
In general, hydrogenation of a derivative adversely affected its compatibility in either the vinyl copolymer or the Buna-N
formulations.
Presented at the 51st annual meeting, American Oil Chemists’ Society, Dallas, Tex., April 4–6, 1960.
One of the laboratories of the Southern Utilization Research and Development Division, Agricultural Research Service, U. S.
Department of Agriculture. 相似文献
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Ewa Langer Sylwia Waśkiewicz Krzysztof Bortel Marta Lenartowicz-Klik Sebastian Jurczyk 《Iranian Polymer Journal》2017,26(2):115-123
In this study, chemical recycling products of waste poly(ethylene terephthalate) with oligoesters were used as new plasticizers for poly(vinyl chloride) (PVC). The preparation conditions of the dry blend mixtures of the suspension PVC containing synthesised plasticizers were similar to the conditions of the preparing mixtures with commercial plasticizers. The plasticization efficiency of PVC plasticizers was then examined by analysis of the mechanical, physical and chemical properties, as well as the thermal resistance and migration of plasticizer molecules from polymer matrix. Test results proved that compositions with synthesised oligomeric plasticizers possessed similar or better properties than those containing commercial oligomeric plasticizers and much better properties than those having monomeric plasticizers. Thermal stabilities of the proposed plasticizers were higher than those of the commercial plasticizers either monomeric (bis(2-ethylhexyl)phthalate) or oligomeric, despite the fact that the synthesised oligoesters did not contain any antioxidant. The best properties, especially low volatility, very good mechanical properties, low migration were resulted of the transesterification of the waste PET with oligoesters based on adipic acid, triethylene glycol and 2-ethylhexanol which were selected as plasticizers synthesised on the technical scale. The tested plasticized PVC compositions possessed very good tear resistance, tensile strength, decrease of weight loss after 168 h at 80 °C and low migration. Processing properties of PVC compositions containing these synthesised plasticizers confirmed their effectiveness in these compositions for extrusion process. 相似文献
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安全玻璃夹层用PVB膜片生产工艺配方的设计 总被引:3,自引:0,他引:3
采用胶片级聚乙烯醇缩丁醛(PVB)树脂为基础树脂,选用了不同的增塑剂和助剂,制成了夹层玻璃所用的膜片,分析了工艺流程中各原材料对产品质量的影响。实验表明,PVB树脂颗粒须粒径均匀,不同用途的夹层玻璃需选用不同的增塑剂,同时进行相应生产工艺的调整,才能实现稳定连续的生产。 相似文献
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Styrene–butadiene rubber (SBR) vulcanizates were prepared using plasticizers including the four liquid types of styrene–butadiene copolymers (LPSB), polybutadiene (LPB), polyisoprene (LPI), and the hydrogenated polyisoprene (LHPI) as well as the conventional process oil, and their phase‐separated structures and mechanical properties were investigated by differential scanning calorimetry and dynamic mechanical spectroscopy. The phase separation was observed for the SBR vulcanizates when LPI and LHPI were used as the plasticizers, while the LPSB and LPB gave homogeneous structures because of the good miscibility with the SBR. The phase‐separated structure of the SBR vulcanizate prepared using LPI changed to the homogeneous during the thermal aging. We revealed the role of the liquid polymers as the plasticizers in maintaining the physical and mechanical properties of the SBR vulcanizates during the thermal aging process when the plasticizers were miscible to the SBR. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
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This paper describes the use of an extruder for the plastification process of potato starch with glycerol and water as plasticizers. The influence of both plasticizers is expressed in the water absorption index (WAI) and water solubility index (WSI). The amount of water added prior to extrusion is a tool to protect the starch polymers from degradation and to improve the extruder performance. 相似文献
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《Journal of Adhesion Science and Technology》2013,27(2):147-168
SBS rubbers containing different loadings of calcium carbonate and/or silica fillers were surface treated with UV-ozone to improve their adhesion to polyurethane adhesive. The surface modifications produced on the treated filled SBS rubbers have been analyzed by contact angle measurements, ATR-IR spectroscopy, XPS and SEM. The adhesion properties have been evaluated by T-peel strength tests on treated filled SBS rubber/polyurethane adhesive/leather joints. The UV-ozone treatment improved the wettability of all rubber surfaces, and chemical (oxidation) and morphological modifications (roughness, ablation, surface melting) were produced. The increase in the time of UV-ozone treatment to 30 min led to surface cleaning (removal of silicon-based moieties) due to ablation and/or melting of rubber layers and also incorporation of more oxidized moieties was produced. Although chemical modifications were produced earlier in an unfilled rubber for short time of treatment with UV-ozone, they were more noticeable in filled rubbers for extended length of treatment, mainly for S6S and S6T rubbers containing silica filler. The oxidation process seemed to be inhibited for S6C and S6T rubbers (containing calcium carbonate filler). On the other hand, the S6S rubber containing silica filler and the lowest filler loading showed the higher extent of modification as a consequence of the UV-ozone treatment. The UV-ozone increased the joint strength in all joints, more noticeably in the rubbers containing silica filler, in agreement with the greater extents of chemical and morphological modifications produced by the treatment in these rubbers. Finally, the nature and content of fillers determined the extent of surface modification and adhesion of SBS rubber treated with UV-ozone. 相似文献